Canonical Allele Identifier: CA931394969
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs548482389
gnomAD v3: 10-94852444-C-G
gnomAD v4: 10-94852444-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852444C>G , CM000672.2:g.94852444C>G GRCh38
NC_000010.10:g.96612201C>G , CM000672.1:g.96612201C>G GRCh37
NC_000010.9:g.96602191C>G NCBI36
NG_008384.2:g.94739C>G
NG_008384.3:g.94764C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1292-289C>G MANE Select ENSP00000360372.3:n.1292-289C>G
ENST00000645461.1:n.2203-289C>G
ENST00000371321.7:c.1292-289C>G ENSP00000360372.3:n.1292-289C>G
ENST00000464755.1:c.2055-289C>G ENSP00000483243.1:n.2055-289C>G
NM_000769.2:c.1292-289C>G NP_000760.1:n.1292-289C>G
NM_000769.4:c.1292-289C>G MANE Select NP_000760.1:n.1292-289C>G
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